N-(2-碘乙基)三氯乙酰胺 ,67680-56-2 _ChemCD

N-(2-碘乙基)三氯乙酰胺

basic_info
Product_Name：	N-(2-碘乙基)三氯乙酰胺
CAS：	67680-56-2
中文同义词：	N-(2-碘乙基)三氯乙酰胺
EnglishSynonyms：	N-(IODOETHYL)TRIFLUOROACETAMIDE ; N-(2-IODOETHYL)TRIFLUORO-ACETAMIDE ; 1-IODO-2-(TRIFLUOROACETYL)AMINOETHANE ; 2,2,2-TRIFLUORO-N-(2-IODOETHYL)ACETAMIDE ; AMINOETHYL-8(TM) REAGENT ; AMINOETHYL-8
pro_mdlNumber：	MFCD00038354
pro_acceptors：	2
pro_donors：	1
pro_smile：	C(CI)NC(=O)C(F)(F)F
InChi：	InChI=1S/C4H5F3INO/c5-4(6,7)3(10)9-2-1-8/h1-2H2,(H,9,10)
InChiKey：	InChIKey=QFRHEHPVTSCSIH-UHFFFAOYSA-N
property
Comments：	A STABLE NON-POLYMERIZING SUBSTITUTE FOR ETHYLENE IMINE FEATURES/BENEFITS: AMINOETHYL-8(TM) REAGENT IS A ONE-STEP MODIFICATION AGENT FOR THE SULFHYDRYL GROUP OF CYSTEINE FEATURES/BENEFITS: AT PH 8.1-8.6, THE SULFHYDRYL GROUP IS AMINOETHYLATED AND THE TRIFLUOROACETYL GROUP IS HYDROLYZED FEATURES/BENEFITS: ONE-STEP MODIFICATION REAGENT FOR SULFHYDRYL GROUPS FEATURES/BENEFITS: THE TRYPSIN SUSCEPTIBLE DERIVATIVE, S-(BETA-AMINOETHYL)CYSTEINE, RESULTS FROM THE REACTION FEATURES/BENEFITS: UNDER THE CONDITIONS OF THE ALKYLATION REACTION, THE -SH GROUP IS ETHYLATED AND THE TRIFLUOROACETYL GROUP IS LOST LETS YOU MODIFY FREE SULFHYDRYLS TO PRIMARY AMINES
secure_info

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